Combination therapy with an anti-IL-1β antibody and GAD65 DNA vaccine can reverse recent-onset diabetes in the RIP-GP mouse model

  1. Matthias G. von Herratha,#
  1. aType 1 Diabetes Center, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, California, United States, 92037.
  2. bCurrent address: Ambrx, Inc. 10975 N Torrey Pines Rd, San Diego, CA 92121.
  1. #Corresponding author: Matthias von Herrath, Email: matthias{at}liai.org

Abstract

Type 1 diabetes is thought to be an autoimmune condition in which self-reactive T cells attack insulin-secreting pancreatic β-cells. As a proinflammatory cytokine produced by β-cells or macrophages, interleukin (IL)-1β represents a potential therapeutic target in diabetes. We reasoned IL-1β blockade could be combined with islet antigen-specific approaches involving glutamic acid decarboxylase of 65kDa (GAD65)-expressing plasmids, as previously shown in combination therapies (CT) with anti-CD3. Thus, we investigated whether anti-IL-1β antibody alone or combined with GAD65 vaccine could reverse diabetes development in a virus-induced mouse model. Given alone, anti-IL-1β had no effect on diabetes while GAD65 plasmid resulted in 33% disease reversal after 5-week observation. However, CT cured 53% of animals and prevented worsening of glycemic control in non-protected individuals for up to 12 weeks. While the GAD65 vaccine arm of the CT was associated with increased Foxp3+ regulatory T-cell frequency in pancreatic lymph nodes, islet infiltration by CD11b+/high cells was less frequent upon CT and its extent correlated with treatment success or failure. Altogether, our CT provided prolonged improvement of clinical and immunological features. Despite unsuccessful clinical trials using anti-IL-1β monotherapy, these data hold promise for treatment of type 1 diabetic patients with IL-1β blockade combined with antigen-specific vaccines.

  • Received August 15, 2013.
  • Accepted February 3, 2014.

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